Aluminium lithium hydride → 1-(Thieno[3,2-c]pyridin-2-yl)ethan-1-ol
反応式
[S:1]1[C:9]2[CH:8]=[CH:7][N:6]=[CH:5][C:4]=2[CH:3]=[C:2]1[C:10](=[O:12])[CH3:11].[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[S:1]1[C:9]2[CH:8]=[CH:7][N:6]=[CH:5][C:4]=2[CH:3]=[C:2]1[CH:10]([OH:12])[CH3:11]参加物
4
実験手順
To a solution of 1-(thieno[3,2-c]pyridin-2-yl)ethanone (D′-3) (3.5 g, 1 mmol) in anhydrous THF (50 mL) was added LiAlH4 (1.13 g, 1.5 mmol) in portions at 0° C. The suspension was stirred under this temperature for 1 h. The reaction mixture was quenched with saturated aqueous NH4Cl solution and filtered. The filtrate was washed with brine, concentrated, and then used for the next step without any further purification.
後処理
- customThe reaction mixture was quenched with saturated aqueous NH4Cl solution
- filtrationfiltered
- washThe filtrate was washed with brine
- concentrationconcentrated
- customused for the next step without any further purification
出典と根拠
- ORDレコード
- ord-596329c447e34f76b860f4f8ff482604
- 出典データセット
- uspto-grants-2013_08
- 特許番号
- US08507487B2
反応ノート
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